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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351665Generated: October 30, 2026

Morpholine → 4-[(5-Bromofuran-2-yl)methyl]morpholine

https://huagongshe.com/reaction/351665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromofuran-2-carbaldehydeHCID 600328—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Product4-[(5-Bromofuran-2-yl)methyl]morpholineHCID 1247868784%

Reaction Steps

To a mixture of 5-bromo-2-furaldehyde (1.76 g) and morpholine (1.00 ml) in 40 mL anhydrous THF at room temperature was added acetic acid (0.60 mL) followed by sodium triacetoxyborohydride (3.28 g). The mixture was stirred at room temperature for 3 h and then poured into a saturated solution of sodium bicarbonate (100 mL). After stirring vigorously for 5 min the layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4), filtered and evaporated to dryness. Purification of the residue by flash chromatography afforded 2.09 g (8.49 mmol, 84% yield) of 4-(5-bromo-2-furylmethyl)morpholine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743788B2
Source datasetuspto-grants-2004_06
ORD IDord-0d078e7e718d4c51a04a92afc91cbe12
Source noteuspto-grants-2004_06